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100986-86-5 molecular structure
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(2R)-7-fluoro-2-methyl-6-(4-methylpiperazin-1-yl)-10-oxo-4-oxa-1-azatricyclo[7.3.1.0^{5,13}]trideca-5(13),6,8,11-tetraene-11-carboxylic acid

ChemBase ID: 2739
Molecular Formular: C18H20FN3O4
Molecular Mass: 361.3675032
Monoisotopic Mass: 361.14378436
SMILES and InChIs

SMILES:
C[C@@H]1COc2c(N3CCN(C)CC3)c(F)cc3c2n1cc(C(=O)O)c3=O
Canonical SMILES:
CN1CCN(CC1)c1c(F)cc2c3c1OC[C@H](n3cc(c2=O)C(=O)O)C
InChI:
InChI=1S/C18H20FN3O4/c1-10-9-26-17-14-11(16(23)12(18(24)25)8-22(10)14)7-13(19)15(17)21-5-3-20(2)4-6-21/h7-8,10H,3-6,9H2,1-2H3,(H,24,25)/t10-/m1/s1
InChIKey:
GSDSWSVVBLHKDQ-SNVBAGLBSA-N

Cite this record

CBID:2739 http://www.chembase.cn/molecule-2739.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
(2R)-7-fluoro-2-methyl-6-(4-methylpiperazin-1-yl)-10-oxo-4-oxa-1-azatricyclo[7.3.1.0^{5,13}]trideca-5(13),6,8,11-tetraene-11-carboxylic acid
(2R)-7-fluoro-2-methyl-6-(4-methylpiperazin-1-yl)-10-oxo-4-oxa-1-azatricyclo[7.3.1.05,13]trideca-5(13),6,8,11-tetraene-11-carboxylic acid
IUPAC Traditional name
@dextrofloxacine
dextrofloxacine
Synonyms
Dextrofloxacine
(2R)-7-fluoro-2-methyl-6-(4-methylpiperazin-1-yl)-10-oxo-4-oxa-1-azatricyclo[7.3.1.0^{5,13}]trideca-5(13),6,8,11-tetraene-11-carboxylic acid
(3R)-9-Fluoro-2,3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic Acid
(+)-Ofloxacin
(R)-(+)-Ofloxacin
D-Ofloxacin
DR 3354
d-Levofloxacin
(R)-Ofloxacin
CAS Number
100986-86-5
MDL Number
MFCD00869643
PubChem SID
160966187
46506037
PubChem CID
452723

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem ALOGPS 2.1
Acid pKa 5.4470572  H Acceptors
H Donor LogD (pH = 5.5) 0.616237 
LogD (pH = 7.4) -0.2825112  Log P 0.65427977 
Molar Refractivity 94.9359 cm3 Polarizability 34.82272 Å3
Polar Surface Area 73.32 Å2 Rotatable Bonds
Lipinski's Rule of Five true 
Log P -0.02  LOG S -2.4 
Solubility (Water) 1.44e+00 g/l 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Hydrophobicity(logP)
-0.508 expand Show data source
MSDS Link
Download expand Show data source
Purity
95% expand Show data source
Certificate of Analysis
Download expand Show data source

DETAILS

DETAILS

DrugBank DrugBank TRC TRC
DrugBank - DB03034 external link
Item Information
Drug Groups experimental
Description A synthetic fluoroquinolone (FLUOROQUINOLONES) antibacterial agent that inhibits the supercoiling activity of bacterial DNA GYRASE, halting DNA REPLICATION. [PubChem]
Toronto Research Chemicals - O245740 external link
Fluorinated quinolone antibacterial. An enantiomer of Levofloxacin (L360000).

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • • Hwangbo, H.J. et al.: Eur. J. Pharmac. Sci., 18, 197 (203)
  • • Gascon, A.R. et al.: J. Clin. Pharmacol, 40, 869 (203)
  • • Monk, J.P., et al.: Drugs, 33, 346 (203)
  • • Drlica, K., Curr. Opin. Microbiol. 2, 504 (203)
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PATENTS

PATENTS

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INTERNET

INTERNET

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